RU2005123810A - METHOD OF DATERING - Google Patents

METHOD OF DATERING Download PDF

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Publication number
RU2005123810A
RU2005123810A RU2005123810/04A RU2005123810A RU2005123810A RU 2005123810 A RU2005123810 A RU 2005123810A RU 2005123810/04 A RU2005123810/04 A RU 2005123810/04A RU 2005123810 A RU2005123810 A RU 2005123810A RU 2005123810 A RU2005123810 A RU 2005123810A
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RU
Russia
Prior art keywords
catalyst
palladium
activated
group
deuteration
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RU2005123810/04A
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Russian (ru)
Inventor
Нобухиро ИТО (JP)
Нобухиро ИТО
Цунеаки МАЕСАВА (JP)
Цунеаки МАЕСАВА
Казусиге МУТО (JP)
Казусиге МУТО
Косаку ХИРОТА (JP)
Косаку ХИРОТА
Хиронао САДЗИКИ (JP)
Хиронао САДЗИКИ
Original Assignee
Вако Пьюр Кемикал Индастриз, Лтд. (Jp)
Вако Пьюр Кемикал Индастриз, Лтд.
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Application filed by Вако Пьюр Кемикал Индастриз, Лтд. (Jp), Вако Пьюр Кемикал Индастриз, Лтд. filed Critical Вако Пьюр Кемикал Индастриз, Лтд. (Jp)
Publication of RU2005123810A publication Critical patent/RU2005123810A/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/36Systems containing two condensed rings the rings having more than two atoms in common
    • C07C2602/42Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/56Ring systems containing bridged rings
    • C07C2603/58Ring systems containing bridged rings containing three rings
    • C07C2603/60Ring systems containing bridged rings containing three rings containing at least one ring with less than six members
    • C07C2603/66Ring systems containing bridged rings containing three rings containing at least one ring with less than six members containing five-membered rings
    • C07C2603/68Dicyclopentadienes; Hydrogenated dicyclopentadienes

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Claims (12)

1. Способ дейтерирования соединения, представленного общей формулой [1]1. A method of deuterating a compound represented by the general formula [1] R1-X-R2 [1],R 1 -XR 2 [1], в которой R1 представляет собой алкильную группу или аралкильную группу, которая может содержать углерод-углеродную двойную и/или тройную связь; R2 представляет собой алкильную группу, которая может содержать углерод-углеродную двойную и/или тройную связь, арильную группу, аралкильную группу, алкоксигруппу, арилоксигруппу или гидроксильную группу; X представляет собой карбонильную группу или гидроксиметиленовую группу; R1 и R2 могут образовывать алициклическое кольцо с атомом углерода, который содержится в Х; при условии, что R2 представляет собой алкильную группу, которая может содержать углерод-углеродную двойную связь и/или тройную связь, арильную группу или аралкильную группу, когда Х представляет собой гидроксиметиленовую группу,in which R 1 represents an alkyl group or an aralkyl group, which may contain a carbon-carbon double and / or triple bond; R 2 represents an alkyl group which may contain a carbon-carbon double and / or triple bond, an aryl group, an aralkyl group, an alkoxy group, an aryloxy group or a hydroxyl group; X represents a carbonyl group or a hydroxymethylene group; R 1 and R 2 can form an alicyclic ring with a carbon atom, which is contained in X; with the proviso that R 2 is an alkyl group which may contain a carbon-carbon double bond and / or triple bond, an aryl group or an aralkyl group when X is a hydroxymethylene group, включающий взаимодействие соединения, представленного общей формулой [1], с источником тяжелого водорода в присутствии активированного катализатора, выбранного из палладиевого катализатора, платинового катализатора, родиевого катализатора, рутениевого катализатора, никелевого катализатора и кобальтового катализатора.comprising reacting a compound represented by the general formula [1] with a source of heavy hydrogen in the presence of an activated catalyst selected from a palladium catalyst, a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst, and a cobalt catalyst. 2. Способ дейтерирования по п.1, в котором Х в общей формуле [1] представляет собой карбонильную группу.2. The deuteration method according to claim 1, in which X in the General formula [1] represents a carbonyl group. 3. Способ дейтерирования по п.1, в котором Х в общей формуле [1] представляет собой гидроксиметиленовую группу.3. The deuteration method according to claim 1, in which X in the General formula [1] represents a hydroxymethylene group. 4. Способ дейтерирования по п.1, в котором источником тяжелого водорода является дейтерированный растворитель.4. The method of deuteration according to claim 1, in which the source of heavy hydrogen is a deuterated solvent. 5. Способ дейтерирования по п.4, в котором дейтерированный растворитель представляет собой оксид дейтерия (D2O).5. The deuteration method according to claim 4, in which the deuterated solvent is deuterium oxide (D 2 O). 6. Способ дейтерирования по п.1, в котором активированный катализатор, выбранный из палладиевого катализатора, платинового катализатора, родиевого катализатора, рутениевого катализатора, никелевого катализатора и кобальтового катализатора, представляет собой катализатор, полученный активацией неактивированного катализатора, выбранного из палладиевого катализатора, платинового катализатора, родиевого катализатора, рутениевого катализатора, никелевого катализатора и кобальтового катализатора, путем контактирования с газообразным водородом или газообразным тяжелым водородом.6. The deuteration method according to claim 1, wherein the activated catalyst selected from a palladium catalyst, a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst, and a cobalt catalyst is a catalyst obtained by activating an inactive catalyst selected from a palladium catalyst, a platinum catalyst , rhodium catalyst, ruthenium catalyst, nickel catalyst and cobalt catalyst, by contacting with gaseous hydrogen or gaseous heavy hydrogen. 7. Способ дейтерирования по п.6, в котором контактирование неактивированного катализатора, выбранного из палладиевого катализатора, платинового катализатора, родиевого катализатора, рутениевого катализатора, никелевого катализатора и кобальтового катализатора, с газообразным водородом или газообразным тяжелым водородом осуществляют в реакционной системе для дейтерирования.7. The deuteration method according to claim 6, wherein contacting a non-activated catalyst selected from a palladium catalyst, a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst and a cobalt catalyst with hydrogen gas or gaseous heavy hydrogen is carried out in a deuteration reaction system. 8. Способ дейтерирования по п.1, в котором активированный катализатор, выбранный из палладиевого катализатора, платинового катализатора, родиевого катализатора, рутениевого катализатора, никелевого катализатора и кобальтового катализатора, представляет собой катализатор, содержащий активированный катализатор на основе палладия.8. The deuteration method according to claim 1, wherein the activated catalyst selected from a palladium catalyst, a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst, and a cobalt catalyst is a catalyst containing an activated palladium-based catalyst. 9. Способ дейтерирования по п.8, в котором активированный катализатор на основе палладия, представляет собой активированный палладий на угле.9. The deuteration method of claim 8, wherein the activated palladium-based catalyst is activated carbon palladium. 10. Способ дейтерирования по п.8, в котором катализатор, содержащий активированный катализатор на основе палладия, представляет собой катализатор, содержащий активированный палладиевый катализатор и активированный платиновый катализатор.10. The deuteration method of claim 8, wherein the catalyst comprising an activated palladium-based catalyst is a catalyst comprising an activated palladium catalyst and an activated platinum catalyst. 11. Способ дейтерирования по п.1, в котором соединение, представленное общей формулой [1], представляет собой трицикло[5.2.1.02,6]декан-8-ол, и активированный катализатор, выбранный из палладиевого катализатора, платинового катализатора, родиевого катализатора, рутениевого катализатора, никелевого катализатора и кобальтового катализатора, представляет собой катализатор, содержащий палладий на угле и платину на угле.11. The deuteration method according to claim 1, wherein the compound represented by the general formula [1] is a tricyclo [5.2.1.0 2,6 ] decan-8-ol, and an activated catalyst selected from a palladium catalyst, platinum catalyst, rhodium The catalyst, ruthenium catalyst, nickel catalyst, and cobalt catalyst is a catalyst containing palladium on carbon and platinum on coal. 12. Трицикло[5.2.1.02,6]декан-8-ол, в котором степень дейтерирования составляет 60% или больше.12. Tricyclo [5.2.1.0 2.6 ] decan-8-ol, in which the degree of deuteration is 60% or more.
RU2005123810/04A 2002-12-27 2003-11-07 METHOD OF DATERING RU2005123810A (en)

Applications Claiming Priority (2)

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JP2002378932 2002-12-27
JP2002-378932 2002-12-27

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US (1) US20060116535A1 (en)
EP (1) EP1577280A4 (en)
JP (1) JP4396522B2 (en)
KR (1) KR20050089979A (en)
CN (1) CN100384792C (en)
AU (1) AU2003277596A1 (en)
CA (1) CA2511885A1 (en)
RU (1) RU2005123810A (en)
TW (1) TW200413274A (en)
WO (1) WO2004060831A1 (en)

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JP2005097239A (en) * 2003-08-20 2005-04-14 Kyoto Univ Method for preparing deuterated hydrocarbon
JP4839839B2 (en) * 2004-01-23 2011-12-21 和光純薬工業株式会社 Deuteration method using mixed catalyst
JP5549077B2 (en) * 2006-12-01 2014-07-16 和光純薬工業株式会社 Deuteration of alkanes
WO2009005069A1 (en) * 2007-07-05 2009-01-08 Wako Pure Chemical Industries, Ltd. Method of deuteration using ruthenium catalyst
CN102020522A (en) * 2009-09-21 2011-04-20 陈松源 Preparation method and application of deuterated drugs
CN102574753B (en) * 2009-10-26 2015-07-08 E.I.内穆尔杜邦公司 Method for preparing deuterated aromatic compounds
WO2011129314A1 (en) * 2010-04-13 2011-10-20 和光純薬工業株式会社 Process for deuteration or tritiation of saccharide
CN103702961A (en) * 2011-05-23 2014-04-02 赛诺菲 Process for the preparation of deuterated compounds containing n-alkyl groups
HUP1200411A2 (en) 2012-07-06 2014-08-28 Debreceni Egyetem Method for the activation of the c-h binding of organic compounds and the system therefor
CN105101792A (en) * 2013-03-15 2015-11-25 杜特里亚农用化学品有限责任公司 Deuterium-enriched aldehydes
AU2013406429B2 (en) * 2013-11-29 2017-09-21 KIM, No Eul Plastic hot water boiler
JP7048976B2 (en) * 2015-11-23 2022-04-06 レトロトップ、 インコーポレイテッド Site-specific isotope labeling of 1,4-diene system
CN109422731A (en) * 2017-08-24 2019-03-05 正大天晴药业集团股份有限公司 Deuterated quinoline
CN111039767B (en) * 2018-10-12 2022-05-24 中国人民大学 Method for preparing deuterated aldehyde by using triazole carbene as catalyst
KR101978651B1 (en) * 2018-10-30 2019-05-15 머티어리얼사이언스 주식회사 Method for preparing deuterated orgarnic compounds and deuterated orgarnic compounds produced by the same
EP4107163A4 (en) 2020-02-21 2024-06-19 Retrotope, Inc. Processes for isotopic modification of polyunsaturated fatty acids and derivatives thereof
CN112778072A (en) * 2020-12-31 2021-05-11 徐州亚兴医疗科技有限公司 Catalytic production process of deuterated benzene
CN113499771B (en) * 2021-09-09 2021-12-07 苏州欣诺科生物科技有限公司 Ruthenium-carbon catalyst and preparation method and application thereof

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AU2003277596A1 (en) 2004-07-29
CA2511885A1 (en) 2004-07-22
US20060116535A1 (en) 2006-06-01
TW200413274A (en) 2004-08-01
EP1577280A1 (en) 2005-09-21
WO2004060831A1 (en) 2004-07-22
JP4396522B2 (en) 2010-01-13
CN100384792C (en) 2008-04-30
JPWO2004060831A1 (en) 2006-05-11
KR20050089979A (en) 2005-09-09
CN1732135A (en) 2006-02-08
EP1577280A4 (en) 2006-08-23

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